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Orally administrated D-arginine exhibits higher enrichment in the brain and milk than L-arginine in ICR mice
D-Amino acids exert various physiological functions and are widely present in animals. However, they are absorbed to a lesser extent than L-amino acids. Little is known about D-arginine (D-Arg); however, its isomer L-Arg serves as a substrate for several metabolites and exhibits various functions in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118480/ https://www.ncbi.nlm.nih.gov/pubmed/31932535 http://dx.doi.org/10.1292/jvms.19-0630 |
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author | ASO, Kenta NISHIGAWA, Takuma NAGAMACHI, Satsuki TAKAKURA, Mayumi FURUSE, Mitsuhiro |
author_facet | ASO, Kenta NISHIGAWA, Takuma NAGAMACHI, Satsuki TAKAKURA, Mayumi FURUSE, Mitsuhiro |
author_sort | ASO, Kenta |
collection | PubMed |
description | D-Amino acids exert various physiological functions and are widely present in animals. However, they are absorbed to a lesser extent than L-amino acids. Little is known about D-arginine (D-Arg); however, its isomer L-Arg serves as a substrate for several metabolites and exhibits various functions including promotion of growth hormone secretion. Milk is the only nutrient source for infants; it plays an important role during their initial growth and brain development. No studies have evaluated the availability of D-Arg in the brain and milk in mammals. Here, we have studied the differential availability of orally administered D- and L-Arg in the brain and milk using ICR mice. Our results revealed that without D-Arg administration, D-Arg was undetectable in both plasma and brain samples. However, the plasma D-Arg was about twice the concentration of L-Arg post administration of the same. In the cerebral cortex and hypothalamus, L-Arg concentration remained almost constant for over period of 90 min after L-Arg treatment. Nevertheless, the L-Arg concentration decreased after D-Arg administration with time compared to the case post L-Arg administration. Contrastingly, D-Arg level sharply increased at both the brain regions with time after D-Arg treatment. Furthermore, L-Arg concentration in the milk hardly increased after L-Arg administration. Interestingly, oral administration of D-Arg showed efficient enrichment of D-Arg in milk, compared with L-Arg. Thus, our results imply that D-Arg may be available for brain development and infant nourishment through milk as an oral drug and/or nutrient supplement. |
format | Online Article Text |
id | pubmed-7118480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71184802020-04-08 Orally administrated D-arginine exhibits higher enrichment in the brain and milk than L-arginine in ICR mice ASO, Kenta NISHIGAWA, Takuma NAGAMACHI, Satsuki TAKAKURA, Mayumi FURUSE, Mitsuhiro J Vet Med Sci Physiology D-Amino acids exert various physiological functions and are widely present in animals. However, they are absorbed to a lesser extent than L-amino acids. Little is known about D-arginine (D-Arg); however, its isomer L-Arg serves as a substrate for several metabolites and exhibits various functions including promotion of growth hormone secretion. Milk is the only nutrient source for infants; it plays an important role during their initial growth and brain development. No studies have evaluated the availability of D-Arg in the brain and milk in mammals. Here, we have studied the differential availability of orally administered D- and L-Arg in the brain and milk using ICR mice. Our results revealed that without D-Arg administration, D-Arg was undetectable in both plasma and brain samples. However, the plasma D-Arg was about twice the concentration of L-Arg post administration of the same. In the cerebral cortex and hypothalamus, L-Arg concentration remained almost constant for over period of 90 min after L-Arg treatment. Nevertheless, the L-Arg concentration decreased after D-Arg administration with time compared to the case post L-Arg administration. Contrastingly, D-Arg level sharply increased at both the brain regions with time after D-Arg treatment. Furthermore, L-Arg concentration in the milk hardly increased after L-Arg administration. Interestingly, oral administration of D-Arg showed efficient enrichment of D-Arg in milk, compared with L-Arg. Thus, our results imply that D-Arg may be available for brain development and infant nourishment through milk as an oral drug and/or nutrient supplement. The Japanese Society of Veterinary Science 2020-01-14 2020-03 /pmc/articles/PMC7118480/ /pubmed/31932535 http://dx.doi.org/10.1292/jvms.19-0630 Text en ©2020 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Physiology ASO, Kenta NISHIGAWA, Takuma NAGAMACHI, Satsuki TAKAKURA, Mayumi FURUSE, Mitsuhiro Orally administrated D-arginine exhibits higher enrichment in the brain and milk than L-arginine in ICR mice |
title | Orally administrated D-arginine exhibits higher enrichment in the brain and
milk than L-arginine in ICR mice |
title_full | Orally administrated D-arginine exhibits higher enrichment in the brain and
milk than L-arginine in ICR mice |
title_fullStr | Orally administrated D-arginine exhibits higher enrichment in the brain and
milk than L-arginine in ICR mice |
title_full_unstemmed | Orally administrated D-arginine exhibits higher enrichment in the brain and
milk than L-arginine in ICR mice |
title_short | Orally administrated D-arginine exhibits higher enrichment in the brain and
milk than L-arginine in ICR mice |
title_sort | orally administrated d-arginine exhibits higher enrichment in the brain and
milk than l-arginine in icr mice |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118480/ https://www.ncbi.nlm.nih.gov/pubmed/31932535 http://dx.doi.org/10.1292/jvms.19-0630 |
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